| Primary Device ID | 15050474520704 |
| NIH Device Record Key | 8fad3012-31bd-41ec-8665-4369b9d42402 |
| Commercial Distribution Status | In Commercial Distribution |
| Version Model Number | OM271000 |
| Catalog Number | OM271000 |
| Company DUNS | 103021940 |
| Company Name | JOHNSON & JOHNSON SURGICAL VISION, INC. |
| Device Count | 1 |
| DM Exempt | true |
| Pre-market Exempt | false |
| MRI Safety Status | Labeling does not contain MRI Safety Information |
| Human Cell/Tissue Product | false |
| Device Kit | false |
| Device Combination Product | false |
| Single Use | true |
| Lot Batch | true |
| Serial Number | false |
| Manufacturing Date | true |
| Expiration Date | true |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | false |
| RX Perscription | true |
| OTC Over-The-Counter | false |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 05050474520707 [Primary] |
| GS1 | 15050474520704 [Package] Contains: 05050474520707 Package: [48 Units] In Commercial Distribution |
| HQC | Unit, phacofragmentation |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 3 |
| Public Version Date | 2020-02-26 |
| Device Publish Date | 2019-04-01 |
| 05050474755093 - HEALON ENDOCOAT PRO | 2025-08-28 HEALON ENDOCOAT PRO 0,85 ML USA |
| 05050474755116 - HEALON DUET PRO II | 2025-08-28 HEALON DUET PRO II US |
| 05050474829572 - SMARTLOAD | 2025-05-21 SMARTLOAD TECNIS EYHANCE US IOL 5.0D |
| 05050474829589 - SMARTLOAD | 2025-05-21 SMARTLOAD TECNIS EYHANCE US IOL 5.5D |
| 05050474829596 - SMARTLOAD | 2025-05-21 SMARTLOAD TECNIS EYHANCE US IOL 6.0D |
| 05050474829602 - SMARTLOAD | 2025-05-21 SMARTLOAD TECNIS EYHANCE US IOL 6.5D |
| 05050474829619 - SMARTLOAD | 2025-05-21 SMARTLOAD TECNIS EYHANCE US IOL 7.0D |
| 05050474829626 - SMARTLOAD | 2025-05-21 SMARTLOAD TECNIS EYHANCE US IOL 7.5D |